Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3008723337.
Observations13
Issue DateOctober 29, 2015
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections2
Establishment Details
Firm
RX South DBA RX3 Compounding Pharmacy LLC
Issued To
RxSouth, LLC (dba RX3 Pharmacy)
Location
Chester, Virginia, United States
FEI Number
3008723337
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
October 29, 2015
Country
United States
Inspection History, 2012 to 2014
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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